Atomfair 2,5-Dibromo-3-methylthiophene C5H4Br2S

Description 2,5-Dibromo-3-methylthiophene (CAS No. 13191-36-1) is a high-purity brominated thiophene derivative with the molecular formula C5H4Br2S . This compound is a valuable intermediate in organic synthesis, particularly in the development of conjugated polymers, pharmaceuticals, and agrochemicals. Its rigid thiophene backbone and bromine substituents make it an excellent building block for cross-coupling reactions such as Suzuki, Stille, and Negishi couplings. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers in materials science, medicinal chemistry, and catalysis.

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Description

Description

2,5-Dibromo-3-methylthiophene (CAS No. 13191-36-1) is a high-purity brominated thiophene derivative with the molecular formula C5H4Br2S. This compound is a valuable intermediate in organic synthesis, particularly in the development of conjugated polymers, pharmaceuticals, and agrochemicals. Its rigid thiophene backbone and bromine substituents make it an excellent building block for cross-coupling reactions such as Suzuki, Stille, and Negishi couplings. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers in materials science, medicinal chemistry, and catalysis.

  • CAS No: 13191-36-1
  • Molecular Formula: C5H4Br2S
  • Molecular Weight: 255.96
  • Exact Mass: 255.83800
  • Monoisotopic Mass: 253.84005
  • IUPAC Name: 2,5-dibromo-3-methylthiophene
  • SMILES: CC1=C(SC(=C1)Br)Br
  • Synonyms: 2,5-Dibromo-3-methylthiophene, 13191-36-1, Thiophene, 2,5-dibromo-3-methyl-, EINECS 236-147-4, DTXSID40157249

Application

2,5-Dibromo-3-methylthiophene is widely used as a monomer in the synthesis of conductive polymers for organic electronics, including OLEDs and OFETs. It serves as a key precursor in pharmaceutical research for the development of thiophene-based bioactive molecules. The compound’s bromine groups also facilitate its use in metal-catalyzed coupling reactions to construct complex heterocyclic frameworks.

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